
Stop by booth #11 to ask questions, chat about your needs, or learn how you can reduce clinical trial times by 20% or more!
Are you looking for some one-on-one time at our booth? Click here to request time with one of our experts at the event.
Session 1
Speaker: Michelle longmire
Date/Time: Monday, November 7th, 10am-10:30am
Title: "Executing on the Mission in a Challenging Market"
Date/Time: Monday, November 7th, 10am-10:30am
Title: "Executing on the Mission in a Challenging Market"
Join us for Michelle Longmire’s keynote panel at the DTRA Annual Meeting on "Executing on the Mission in a Challenging Market" on the morning of Monday Nov 7th at the Encore resort in Boston.
Panelist: Michelle Longmire, Medable, Kim Boericke, Thread, & Stuart Redding, MRN
Session 2
Speaker: Mohammed Ali
Date/Time: Monday, November 7th, 2:20 PM - 2:35 PM
Title: "Shaping the future of clinical trial development with a Patient-First Approach"
Date/Time: Monday, November 7th, 2:20 PM - 2:35 PM
Title: "Shaping the future of clinical trial development with a Patient-First Approach"

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Expand Global Access to Trials
Accessible on any web-enabled device (BYOD or provisioned), our scalable solution can inform and consent participants anywhere in the world. Flexible enough for any country or site, you can easily collect compliant signatures (digital or wet-ink), on-site or remote with integrated TeleVisit.
Improve Participant Retention
Deliver an engaging, informational experience for your participants and their caregivers with an easy-to-follow web-based app, featuring explainer videos, interactive diagrams, optional self-assessments and more.
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Minimize Compliance Errors
Gain complete visibility and oversight into your trial with real-time monitoring of all consent activities within a single dashboard and ensure inspection-ready audit trails with fully integrated template management and version control.

Self-service authoring tool to easily create engaging consent templates

Biosample attribution to confirm storage permissions for consent objects

Permission-based workflows by roles and responsibilities for secure control

Compliant with FDA 21 CFR Part 11, eIDAS, HIPAA, GDPR, and ICH GCP


Andrew Mackinnon
Vice President and General Manager eConsent and Digital Solutions
Designed by Trial Experts
Our team of experts will partner with you to determine the best approach for your unique consent needs. Schedule a call to learn more about our scalable, web-enabled tools to level up your consent process.